Canonical Allele Identifier: CA454608499

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44187251C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147652C>T , CM000669.2:g.44147652C>T	GRCh38
NC_000007.13:g.44187251C>T , CM000669.1:g.44187251C>T	GRCh37
NC_000007.12:g.44153776C>T	NCBI36
NG_008847.1:g.46772G>A
NG_008847.2:g.55519G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*859G>A	ENSP00000379142.4:n.*859G>A
ENST00000616242.5:c.853+8G>A	ENSP00000482149.2:n.853+8G>A
ENST00000345378.7:c.864G>A	ENSP00000223366.2:p.Gln288=
ENST00000403799.8:c.861G>A MANE Select	ENSP00000384247.3:p.Gln287=
ENST00000671824.1:c.853+8G>A	ENSP00000500264.1:n.853+8G>A
ENST00000673284.1:c.861G>A	ENSP00000499852.1:p.Gln287=
ENST00000345378.6:c.864G>A	ENSP00000223366.2:p.Gln288=
ENST00000395796.7:c.858G>A	ENSP00000379142.3:p.Gln286=
ENST00000403799.7:c.861G>A	ENSP00000384247.3:p.Gln287=
ENST00000437084.1:c.810G>A	ENSP00000402840.1:p.Gln270=
ENST00000616242.4:c.858G>A	ENSP00000482149.1:p.Gln286=
NM_000162.3:c.861G>A	NP_000153.1:p.Gln287=
NM_033507.1:c.864G>A	NP_277042.1:p.Gln288=
NM_033508.1:c.858G>A	NP_277043.1:p.Gln286=
NM_000162.4:c.861G>A	NP_000153.1:p.Gln287=
NM_001354800.1:c.861G>A	NP_001341729.1:p.Gln287=
NM_033507.2:c.864G>A	NP_277042.1:p.Gln288=
NM_033508.2:c.858G>A	NP_277043.1:p.Gln286=
NM_000162.5:c.861G>A MANE Select	NP_000153.1:p.Gln287=
NM_033507.3:c.864G>A	NP_277042.1:p.Gln288=
NM_033508.3:c.858G>A	NP_277043.1:p.Gln286=